A Tyr368His RPE65 founder mutation is associated with variable expression and progression of early onset retinal dystrophy in 10 families of a genetically isolated population (Q24676361)
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Current Data About A Tyr368His RPE65 founder mutation is associated with variable expression and progression of early onset retinal dystrophy in 10 families of a genetically isolated population
(P31) (Q13442814)

(P304) 709-13

(P407) (Q1860)

(P433) 9

(P478) 40

(P577) +2003-09-00T00:00:00Z

(P1433) (Q14640281)

(P1476) "A Tyr368His RPE65 founder mutation is associated with variable expression and progression of early onset retinal dystrophy in 10 families of a genetically isolated population" (language: en)

(P2093) S Yzer
(P1545) 1

L I van den Born
(P1545) 2

J Schuil
(P1545) 3

H Y Kroes
(P1545) 4

M M van Genderen
(P1545) 5

F N Boonstra
(P1545) 6

B van den Helm
(P1545) 7

H G Brunner
(P1545) 8

R K Koenekoop
(P1545) 9

F P M Cremers
(P1545) 10

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(P356) 10.1136/JMG.40.9.709
(P698) 12960219
(P932) 1735582
(P5875) 10579136